Burlina AB - Search Results

1

Nutrition in adult patients with selected lysosomal storage diseases.

Carubbi F, Barbato A, Burlina AB, Francini F, Mignani R, Pegoraro E, Landini L, De Danieli G, Bruni S, Strazzullo P; Italian Society of Human Nutrition Working Group on Nutrition in Lysosomal Storage Diseases. Carubbi F, et al. Among authors: burlina ab. Nutr Metab Cardiovasc Dis. 2021 Mar 10;31(3):733-744. doi: 10.1016/j.numecd.2020.11.028. Epub 2020 Dec 9. Nutr Metab Cardiovasc Dis. 2021. PMID: 33589321 Review.

2

Application of the WHOQOL-100 for the assessment of quality of life of adult patients with inherited metabolic diseases.

Cazzorla C, Del Rizzo M, Burgard P, Zanco C, Bordugo A, Burlina AB, Burlina AP. Cazzorla C, et al. Among authors: burlina ab, burlina ap. Mol Genet Metab. 2012 May;106(1):25-30. doi: 10.1016/j.ymgme.2012.02.008. Epub 2012 Feb 16. Mol Genet Metab. 2012. PMID: 22398241

3

Newborn screening for lysosomal storage disorders by tandem mass spectrometry in North East Italy.

Burlina AB, Polo G, Salviati L, Duro G, Zizzo C, Dardis A, Bembi B, Cazzorla C, Rubert L, Zordan R, Desnick RJ, Burlina AP. Burlina AB, et al. Among authors: burlina ap. J Inherit Metab Dis. 2018 Mar;41(2):209-219. doi: 10.1007/s10545-017-0098-3. Epub 2017 Nov 15. J Inherit Metab Dis. 2018. PMID: 29143201

4

Light and Shadows in Newborn Screening for Lysosomal Storage Disorders: Eight Years of Experience in Northeast Italy.

Gragnaniello V, Cazzorla C, Gueraldi D, Puma A, Loro C, Porcù E, Stornaiuolo M, Miglioranza P, Salviati L, Burlina AP, Burlina AB. Gragnaniello V, et al. Among authors: burlina ab. Int J Neonatal Screen. 2023 Dec 25;10(1):3. doi: 10.3390/ijns10010003. Int J Neonatal Screen. 2023. PMID: 38248631 Free PMC article.

5

NADPH oxidase activity and chemotaxis by neutrophils in two patients with glycogen storage disease type Ib treated with recombinant human granulocyte-monocyte colony-stimulating factor.

Piva E, De Toni S, Bovo C, Bordugo A, Burlina AB, Plebani M. Piva E, et al. Among authors: burlina ab. Haematologica. 1996 Mar-Apr;81(2):148-51. Haematologica. 1996. PMID: 8641644

6

Increased plasma biotinidase activity in patients with glycogen storage disease type Ia: effect of biotin supplementation.

Burlina AB, Dermikol M, Mantau A, Piovan S, Grazian L, Zacchello F, Shin Y. Burlina AB, et al. J Inherit Metab Dis. 1996;19(2):209-12. doi: 10.1007/BF01799431. J Inherit Metab Dis. 1996. PMID: 8739967 No abstract available.

7

Long-term follow-up results in enzyme replacement therapy for Pompe disease: a case report.

Del Rizzo M, Fanin M, Cerutti A, Cazzorla C, Milanesi O, Nascimbeni AC, Angelini C, Giordano L, Bordugo A, Burlina AB. Del Rizzo M, et al. Among authors: burlina ab. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S389-93. doi: 10.1007/s10545-010-9195-2. Epub 2010 Sep 10. J Inherit Metab Dis. 2010. PMID: 20830524

8

Metabolic stroke in a late-onset form of isolated sulfite oxidase deficiency.

Del Rizzo M, Burlina AP, Sass JO, Beermann F, Zanco C, Cazzorla C, Bordugo A, Giordano L, Manara R, Burlina AB. Del Rizzo M, et al. Among authors: burlina ab, burlina ap. Mol Genet Metab. 2013 Apr;108(4):263-6. doi: 10.1016/j.ymgme.2013.01.011. Epub 2013 Jan 27. Mol Genet Metab. 2013. PMID: 23414711

9

Enzymes of lysosomal origin in the cerebrospinal fluid and plasma of patients with multiple sclerosis.

Goi G, Caputo D, Bairati C, Lombardo A, Burlina AB, Ferrante P, Cazzullo CL, Tettamanti G. Goi G, et al. Among authors: burlina ab. Eur Neurol. 1993;33(1):1-4. doi: 10.1159/000116888. Eur Neurol. 1993. PMID: 8440277

10

Clinical and biochemical approach to the neonate with a suspected inborn error of amino acid and organic acid metabolism.

Burlina AB, Bonafé L, Zacchello F. Burlina AB, et al. Semin Perinatol. 1999 Apr;23(2):162-73. doi: 10.1016/s0146-0005(99)80048-2. Semin Perinatol. 1999. PMID: 10331467 Review.

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